Job Information

Georgia Employer CLINICAL RESEARCH COORDINATOR PRN in Savannah, Georgia

Description IntroductionDo you have the PRN career opportunities as a Clinical Research Coordinator PRN you want with your current employer? We have an exciting opportunity for you to join Memorial Health University Medical Center which is part of the nation\'s leading provider of healthcare services, HCA Healthcare.BenefitsMemorial Health University Medical Center, offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include:Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as telemedicine services and free AirMed medical transportation.Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.Fertility and family building benefits through ProgynyFree counseling services and resources for emotional, physical and financial wellbeingFamily support, including adoption assistance, child and elder care resources and consumer discounts401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service)Employee Stock Purchase PlanRetirement readiness and rollover services and preferred banking partnershipsEducation assistance (tuition, student loan, certification support, dependent scholarships)Colleague recognition programTime Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence)Note: Eligibility for benefits may vary by location.Our teams are a committed, caring group of colleagues. Do you want to work as aClinical Research Coordinator PRN where your passion for creating positive patient interactions are valued? If you are dedicated to caring for the well-being of others, this could be your next opportunity. We want your knowledge and expertise!Job Summary and Qualifications1. Coordinates the preparation of protocols to be submitted for IRB approval.2. Coordinates the on-going regulatory communication with research base or industry sponsor and local physician(s)3. Coordinates with the Clinical Research Nurse (CRN) in identifying appropriate participants for entry into clinical research protocols4. Coordinates the on-going collection and submission of study dataProtocol Mgt: Develops a thorough familiarity of protocol requirements through: 1) reading the protocol, 2) discussions with the Clinical Research Nurse (CRN) and/or Principal Investigator (PI), and the protocol Sponsor/research base, 3) and by attendance of the sponsor\'s investigator meetings. Provides monthly protocol listings/indexes to all concerned physicians and staff. Coordinates with Investigational pharmacist to obtain any protocol drugs from research base or industry Sponsor for any participant on protocol. Ensures that all information required by the research base is responded to in a timely manner. Reports and documents all serious adverse events to principal investigator (PI), Research Nurse immediately and notifies IRB within 72 hours of becoming... For full info follow application link.We are committed to: Providing an inclusive work environment whereeveryone is treated with fairness, dignity and respect. Recruiting and retaining a diverse staff reflective of the patients and communities we serve. Equal employment opportunities are provided to all employees and applicants for employment without regard to race, color, religion, gender, national origin, citizenship, age, disability, sexual orientation, genetic information, gender identity, protected veteran status, or any other legally protected category in accordance to applicable federal, state, or local laws.